Citation: Ag. Myers et Jk. Barbay, On the inherent instability of alpha-amino alpha '-fluoro ketones. Evidence for their transformation to reactive oxyvinyliminium ion intermediates, ORG LETT, 3(3), 2001, pp. 425-428
Authors:
Myers, AG
Siegel, DR
Buzard, DJ
Charest, MG
Citation: Ag. Myers et al., Synthesis of a broad array of highly functionalized, enantiomerically purecyclohexanecarboxylic acid derivatives by microbial dihydroxylation of benzoic acid and subsequent oxidative and rearrangement reactions, ORG LETT, 3(18), 2001, pp. 2923-2926
Citation: Se. Schaus et al., Gene transcription analysis of Saccharomyces cerevisiae exposed to neocarzinostatin protein-chromophore complex reveals evidence of DNA damage, a potential mechanism of resistance, and consequences of prolonged exposure, P NAS US, 98(20), 2001, pp. 11075-11080
Citation: Ag. Myers et al., Asymmetric synthesis of chiral organofluorine compounds: Use of nonracemicfluoroiodoacetic acid as a practical electrophile and its application to the synthesis of monofluoro hydroxyethylene dipeptide isosteres within a novel series of HIV protease inhibitors, J AM CHEM S, 123(30), 2001, pp. 7207-7219
Citation: Ag. Myers et At. Plowright, Synthesis and evaluation of bishydroquinone derivatives of (-)-saframycin A: Identification of a versatile molecular template imparting potent antiproliferative activity, J AM CHEM S, 123(21), 2001, pp. 5114-5115
Authors:
Myers, AG
Zhong, BY
Kung, DW
Movassaghi, M
Lanman, BA
Kwon, S
Citation: Ag. Myers et al., Synthesis of C-protected alpha-amino aldehydes of high enantiomeric excessfrom highly epimerizable N-protected alpha-amino aldehydes, ORG LETT, 2(21), 2000, pp. 3337-3340
Citation: Ag. Myers et Dw. Kung, One-step construction of the pentacyclic skeleton of saframycin a from a "trimer" of alpha-amino aldehydes, ORG LETT, 2(19), 2000, pp. 3019-3022
Citation: Ag. Myers et Sd. Goldberg, Synthesis of the kedarcidin core structure by a transannular cyclization pathway, ANGEW CHEM, 39(15), 2000, pp. 2732-2735
Citation: Ag. Myers et al., Observations concerning the existence and reactivity of free alpha-amino aldehydes as chemical intermediates: Evidence for epimerization-free adduct formation with various nucleophiles, J AM CHEM S, 122(13), 2000, pp. 3236-3237
Citation: Ag. Myers et Jl. Gleason, Asymmetric synthesis of alpha-amino acids by the alkylation of pseudoephedrine glycinamide: L-allylglycine and N-Boc-L-allylglycine, ORG SYNTH, 76, 1999, pp. 57-76
Citation: Ag. Myers et al., Synthetic replacement of the methylamino group of neocarzinostatin chromophore with hydroxyl prohibits thiol activation in organic solvents and diminishes the rate and efficiency of thiol-promoted DNA cleavage in water, TETRAHEDR L, 40(28), 1999, pp. 5129-5133
Citation: Ag. Myers et al., Greatly simplified procedures for the synthesis of alpha-amino acids by the direct alkylation of pseudoephedrine glycinamide hydrate, J ORG CHEM, 64(9), 1999, pp. 3322-3327
Citation: Ag. Myers et Dw. Kung, A concise, stereocontrolled synthesis of (-)-saframycin A by the directed condensation of alpha-amino aldehyde precursors, J AM CHEM S, 121(46), 1999, pp. 10828-10829
Authors:
Myers, AG
Kung, DW
Zhong, BY
Movassaghi, M
Kwon, S
Citation: Ag. Myers et al., Preparation of chiral, C-protected alpha-amino aldehydes of high optical purity and their use as condensation components in a linear synthesis strategy, J AM CHEM S, 121(36), 1999, pp. 8401-8402
Citation: Ag. Myers et Sd. Goldberg, Concise synthesis of the bicyclic core of the chromoprotein antibiotics kedarcidin and neocarzinostatin by transannular reductive cyclization of a tetrayne precursor., TETRAHEDR L, 39(52), 1998, pp. 9633-9636